The following data is part of a premarket notification filed by Mectron Spa with the FDA for Piezosurgery White.
Device ID | K151248 |
510k Number | K151248 |
Device Name: | PIEZOSURGERY WHITE |
Classification | Drill, Bone, Powered |
Applicant | MECTRON SPA VIA LORETO 15 Carasco, IT 16042 |
Contact | Mr. Franco Zunino |
Correspondent | Mr. Roger Gray Donawa Lifescience Consulting S.r.l. Piazza Albania, 10 Rome, IT 00153 |
Product Code | DZI |
CFR Regulation Number | 872.4120 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-05-11 |
Decision Date | 2015-09-04 |